Radiodiagnosis of dontogenous tumours and non tumoral formations of jaws. Radio diagnosis of non dontogenous benign and malignant tumours and non tumoral

Radiodiagnosis Radiodiagnosis of dontogenous of dontogenous tumours and tumours and non tumoral formations of jawsnon tumoral formations of jaws. . Radio Radio

diagnosis of diagnosis of nonon n dontogenous dontogenous benign andbenign and malignant malignant tumours and non tumoral tumours and non tumoral

formations of jawsformations of jaws..

Prof. G.S. Moroz, MDProf. G.S. Moroz, MD

Department of Oncology & Department of Oncology & Radiology,Radiology,

Ternopil State Medical UniversityTernopil State Medical University

Carotid Body Tumor*Note: The pictures don't correspond with the text of the slides

EtiologyRare neoplasm arising from nonchromaffin paraganglia in

carotid artery bifurcation

Heredofamilial (autosomal-dominant) form can occur (in less

than 10%) Can be multiple,

bilateral, or multicentric

Clinical Presentation

Typically presents as a mass in the lateral neck

May be associated with bruit, hoarseness, dysphagia

Diagnosis

Ultrasonography as a screening measure • Angiography of both carotid systems

Differential Diagnosis

Metastatic tumor • Vagal nerve sheath tumor

Treatment

Surgical removal • Radiation therapy • Combined surgical and radiotherapy

Prognosis

Generally good • Can be locally invasive • May

metastasize in 5 to 25% of cases

Exostosis Etiology

Unknown • Probable reactive Phenomenon (stimulus undetermined)


Asymptomatic, bony, nodular masses • Cortical bone enlargement of the jaws;

usually bilateral and symmetric • Usually multiple; slow growing • Most commonly along buccal/facial

aspects of the maxillary and mandibular alveolar ridge • Overlying mucosa intact, unremarkable • Usually develops in adults

Diagnosis

May appear Radiographicall

y as

homogeneous opacities


Peripheral fibroma • Periostitis • Periosteal/ parosteal osteosarcoma

Treatment

None required • May need to be removed for prosthesis (denture) construction

Prognosis

Excellent

Benign Nonodontogenic Benign Nonodontogenic TumorsTumors

Juvenile Ossifying FibromaEtiology

A rapidly evolving

variant of ossifying fibroma of the young • Cause

unknown


Onset between 5 and 15 years of age

• Rapid growth over several weeks

• Maxilla and paranasal areas predominate

• Tooth displacement common

Radiographic Findings

Well-defined radiolucency • Focal mineralization may be

noted. • Adjacent bone may be eroded

or destroyed.

Microscopic Findings

Prominent stromal cellularity • Woven bone and/or

psammomatous calcifications • Plump osteoblast rimming

Diagnosis

Correlation of histologic and radiographic findings


Osteosarcoma • Central giant cell granuloma • Odontogenic tumor

Treatment

Wide local excision or resection •

Reconstruction

Prognosis

Recurrence rate

of 30 to 50%

Langerhans Cell Disease(Idiopathic Histiocytosis)

Etiology • Unknown • Proliferation of Langerhans’

cells (immune surveillance cells) normally found in skin, mucosa,

bone marrow, and lymph nodes


A broad spectrum, typically divided into three subsets, as follows:

• Unifocal or multifocal chronic disease of bone (eosinophilic granuloma) • Widely disseminated chronic disease of bone and soft tissue (Hand-Schüller-Christian disease) • Acute, disseminated disease with bone marrow involvement (Letterer-Siwe disease) • Most arise in childhood; eosinophilic granuloma often arises

in adolescents and adults. • Jaw lesions noted in up to 20% of cases with tenderness,

loose teeth (focal to segmental), gingival inflammation, and friability


Bone lesions often punched out, sharply circumscribed

• “Floating teeth” appearance with alveolar bone involvement

• Skeletal survey should be performed to rule out multiple bone

involvement

Diagnosis

Radiographic demonstration of lytic bony lesions • Infiltrate of mononuclear cells, often with clefted

nuclei • Often accompanied by a variety of other cell types,

including eosinophils, lymphocytes, giant cells, plasma cells • Immunohistochemical demonstration of CD1a

staining • Langerhans’ cells also stain for S-100 protein,

although the antibody is less specific. • Ultrastructural demonstration of cytoplasmic

racquet-shaped Birbeck granules

Differential Diagnosis: Radiologic

Juvenile periodontitis, endocrinopathies, hypophosphatasia,

leukemia, bony malignancy (primary/metastatic)

• In adults: myeloma

Treatment

Localized variant • Surgical curettage of bony lesions • Low-dose radiation therapy of

inaccessible lesions • Widespread variants • Chemotherapy including

methotrexate, vincristine, cyclophosphamide • Bone marrow transplantation for

resistant/recurrent disease

Prognosis

Varies with form of disease, as follows: • Localized variant: very good • Disseminated variant: fair to poor

Ossifying Fibroma

Etiology • A benign

fibro- osseous lesion of bone • Cause

unknown


Expansile lesion of bone • Cortices intact • May produce deformity,

malocclusion, dysfunction • Mandibular lesions are more

common than are maxillary.


Well-delineated, smooth contours • Quality varies from lucent to

opaque • Margins may be sclerotic. • Can resorb roots and displace

teeth • May displace mandibular canal


Fibrovascular stroma • Islands/trabeculae of osteoid,

woven bone • Cementum droplets may be

present.

Diagnosis

Correlation of histologic and radiographic findings

Differential Diagnosis: Radiographic

Odontogenic cyst

• Giant cell lesion

• Odontogenic tumor

Differential Diagnosis: Histologic

Fibrous dysplasia

(must have clinical-

pathologic correlation)

Treatment

Conservative excision • Enucleation with peripheral bony curettage

Prognosis

Excellent

Osteoma

Etiology • Sporadic form is idiopathic • May be a component of

Gardner’s syndrome • Excludes maxillary and

mandibular tori


Sporadic form with frontal and sphenoid sites predisposed

• May be multiple • Solitary lesions rare in jaws


Well circumscribed,

dense, sclerotic • May be subperiosteal or medullary

Diagnosis

Radiographic features • Microscopic features:

normal cortical and trabecular bone


Tori, exostoses • Ossifying fibroma • Osteoblastoma • Focal

sclerosing osteitis

Treatment

Usually none • Local

resection, if

compromising

Prognosis

Excellent • Little recurrence potential • When associated with Gardner’s

syndrome, malignant conversion of intestinal polyps is assured.

Peripheral Ossifying Fibroma

Etiology • A reactive hyperplasia of the

gingiva; may be related to chronic irritation • Periodontal ligament/membrane

origin postulated


Exclusive gingival location; commonly interdental

• Nodular, sessile to pedunculated, usually ulcerated mass

• Slow growing; may rarely displace teeth • Usually in young adults and adolescents • Early lesions may bleed easily. • Anterior maxillary arch is favored site

Diagnosis

Central islands or trabeculae of bone/cementum

• Fibroblastic proliferation in a sheet-like configuration

• Usually ulcerated with granulation tissue base


Pyogenic granuloma • Peripheral giant cell granuloma • Peripheral fibroma • Peripheral odontogenic tumor • Osteosarcoma/chondrosarcoma • Metastatic neoplasm

Treatment

Excision including

underlying periosteum or associated periodontal ligament

Prognosis

Recurrence occasionally

seen; believed to be related to incomplete excision

Benign Nonodontogenic TumorsBenign Nonodontogenic Tumors

Benign Nonodontogenic TumorsBenign Nonodontogenic Tumors

Malignant NonodontogenicTumors Ewing’s Sarcoma Etiology • Unknown • Chromosomal translocations t(11;22),

t(7;22), t(7;21) noted • Gene rearrangement often noted, that is,

(22;q12) and expression of the MIC2 gene • Genetically related to primitive peripheral

neuroectodermal tumor via translocations


60% in males; over 95% in those under 20 years of age

• Chiefly in bone and soft tissues • Highly malignant • Pain, numbness, and swelling often early complaints • Diffuse, irregular, lytic bone lesion • Cortical expansion variable • Second most common bone tumor of

children/adolescents • Soft tissues of head and neck account for 11% of

extraskeletal sites

Diagnosis

Radiographs often show “moth-eaten” appearance and laminar periosteal bone reaction • Cortex may be eroded or expanded


Osteosarcoma • Lymphoma • Peripheral neuroectodermal

tumor of bone • Primitive rhabdomyosarcoma • Neuroectodermal tumor of

infancy

Treatment

Radiation and multiagent chemotherapy

Prognosis

54 to 74% 5-year survival rate in localized osseous form • Late relapse

not uncommon

Metastatic Cancer

Etiology • Spread of a primary malignancy

to the oral cavity structures or jaws (usually from lung, breast,

prostate, colon, kidney) • Accounts for < 1% of oral

malignancies


Usually manifests in the jaws with pain and swelling

• Not uncommon is loosening of teeth or pathologic jaw fracture

• Soft tissue location is rare. • Most frequent sites of primary

neoplasms are kidney, lung, breast, colon, prostate, stomach • Intraosseous lesions with lytic, ill-

defined radiolucencies


As with the primary tumor • Tumor marker studies

(immunohistochemical) may be necessary

to define the site of origin.

Diagnosis

Radiographic findings • Biopsy


Primary soft tissue tumor • Primary osseous tumor • Periodontitis (localized) •

Osteoradionecrosis

Treatment

Local radiation • Combination chemoradiother

apy

Prognosis

Poor

Malignant Nonodontogenic Malignant Nonodontogenic TumorsTumors

OsteosarcomaEtiology

May be associated with pre-existing bone disease such as the

following: • Paget’s disease (10 to 15%) • Fibrous dysplasia (0.5%) • Mutation/amplification of p53, c-

myc, c-JUN, c-fos, MOM2, CDK4, SAS


May present with pain paresthesia, trismus, nasal or paranasal

sinus obstruction • May masquerade as an odontogenic

infection • Intraoral signs are as follows: • Tooth mobility (vertical) • Periapical radiolucency (teeth vital) • Distal displacement of terminal molar • Jaw mass may be ulcerat


Early intraoral findings • Displacement of teeth • Root resorption • Absent or attenuated lamina dura • Uniformly widened periodontal membrane space • Later jaw bone findings • Lytic, “moth-eaten” destruction • Cortical destruction • Soft tissue extension • Erosion of mandibular canal • 25% of cases have “sunburst effect” (radiating

radiopaque spicules)


Sarcomatous stroma • Osteoid production by neoplastic

cells • Four basic patterns (no

prognostic significance) are as follows:

• Osteoblastic • Fibroblastic • Chondroblastic • Telangiectatic

Diagnosis

Correlation of clinical, radiographic, Pathologic findings


Fibro-osseous lesion • Osteomyelitis •

Osteoradionecrosis • Metastatic tumor • Other form of sarcoma

Treatment

Radical ablative surgery • Hemimandibulectomy • Partial maxillectomy ± orbital

exenteration • Adjuvant

chemotherapy/radiotherapy

Prognosis

Survival ranges from 12 to 58% at 5 years

• Mandibular lesions are associated with a greater survival rate

than are maxillary lesions.

Odontogenic Tumors Odontogenic Tumors Adenomatoid Odontogenic

Tumor

Etiology • Derivation from epithelial

component of the enamel organ • Represents less than 10% of

odontogenic tumors • Biologic behavior allows for

distinction from ameloblastoma


Narrow age range, 5 to 30 years, with most cases noted during

second decade • Female predilection • Anterior jaw location common • Association with unerupted tooth • Asymptomatic; occasionally produces

expansion of alveolar bone • Rarely occurs in gingival soft tissue

(peripheral) • May produce root divergence of adjacent teeth


Well defined, unilocular, often adjacent to crown of unerupted

tooth • Opaque foci may be scattered

within the lucency in a “snowflake” or “salt and pepper”

pattern.


Characteristic intraluminal/intracystic growth with welldefined

capsule • Dual cell population: spindle cells

and cuboidal to columnar cells forming tubules or pseudoducts • Foci of dystrophic calcification or

eosinophilic droplets may be noted.

Diagnosis

Radiographic features • Microscopic findings


Dentigerous cyst • Odontogenic keratocyst • Calcifying odontogenic cyst • Lateral root cyst • Calcifying epithelial

odontogenic tumor

Treatment

Enucleation

Prognosis

No recurrence

Ameloblastic Fibroma andAmeloblastic Fibro-odontoma Etiology • Ameloblastic fibroma: a benign mixed

odontogenic tumor with concomitant epithelial and

mesenchymal neoplastic proliferation • Ameloblastic fibro-odontoma: as for

ameloblastic fibroma with the addition of an odontoma • Spontaneous; no known cause for

either


Noted mostly in first and second decades

• Approximately 70% in mandible, usually posterior region

• No gender predilection • May cause jaw expansion • Asymptomatic


Well defined with hyperostotic margin

• Unilocular to multilocular • Often associated with an

unerupted tooth • Ameloblastic fibro-odontoma has

opaque component(s) related to enamel and dentin in the

odontoma component

Diagnosis

Lobulated, cellular mesenchymal component with proliferating

odontogenic epithelium in cords and islands

• Enamel matrix, dentin formation associated with odontoma

(when present)


Ameloblastoma • Dentigerous cyst • Odontogenic keratocyst • Odontogenic myxoma • Central giant cell granuloma

Treatment

Conservative surgical

excision/ curettage

Prognosis

Excellent

Ameloblastoma

Etiology • A benign, aggressive jaw tumor

of odontogenic epithelial (ectodermal)

origin; the most common odontogenic tumor after the

odontoma • Incidence of 0.3 cases per million

people


Peak incidence during third to fifth decades • 80% occur in the mandible, chiefly in molar

and ramus region • Often presents in association with

unerupted third molar teeth • May produce marked deformity, facial

asymmetry • Extraosseous or peripheral variant arises in

gingival tissues of older adults (fifth to seventh decades) • Typically slow growing, but persistent


Osteolytic or radiolucent with sclerotic, smooth, even borders

• May be unilocular to multilocular • Root resorption or tooth

displacement may be seen. • Can expand affected jaw in any

plane • Cortical perforation may occur.

Diagnosis

Sheets, strands, islands of odontogenic epithelium • Peripheral layer of cuboidal to columnar ameloblast-like

cells enclosing a cell population analogous to stellate reticulum

of the enamel organ • Cystic degeneration common within stellate reticulum

component • Several histologic patterns described have no clinical

relevance. • A biologic variant, cystic (unicystic) ameloblastoma,

occurs in younger patients; has a less aggressive clinical course and

is managed more conservatively • Malignant variants rarely seen


Dentigerous cyst • Odontogenic keratocyst Odontogenic myxoma • Central giant cell granuloma

Treatment

Varies with subtype, size, location • Solid/multicystic lesions

generally require local excision or resection. • The cystic variant requires local

excision, as recurrences may follow curettage only

Prognosis

Generally good; recurrence rates higher with conservative

treatment • Recurrence rates of up to 15%

following marginal resection • Very good prognosis for cystic

ameloblastoma • Long-term follow-up necessary

Calcifying Epithelial Odontogenic Tumor

Etiology • A benign odontogenic tumor of

uncertain histogenesis • Stratum intermedium

component of enamel organ is favored

cell of origin


Chiefly in posterior mandible • Painless, slow growing • Mean age of occurrence is

approximately 40 years • Occasional soft tissue origin

(peripheral) noted as a sessile gingival mass • Jaw expansion a common clinical

presentation


Usually noted in association with an impacted tooth

• Multilocular; most often with mixed radiolucent and

radiopaque features • Impacted tooth often obscured by

tumor-associated calcification • Margins may be well defined or

sclerotic and vague.

Diagnosis

Radiographic features • Biopsy findings of polyhedral

epithelial cells, nuclear pleomorphism,

amyloid material, and concentric calcifications with

epithelial islands


When radiolucency predominates: dentigerous cyst, odontogenic

keratocyst, ameloblastoma, odontogenic myxoma

• With mixed radiolucent and radiopaque features: calcifying

odontogenic cyst, adenomatoid odontogenic tumor, ameloblastic

fibro-odontoma, fibro-osseous lesion, osteoblastoma

Treatment

Local, conservative excision including a thin rim of normal

bone (so-called ostectomy) versus conservative en bloc removal

• Peripheral lesions with a narrow periphery of normal-appearing

mucosa

Prognosis

Very good • Recurrence rate is low, from 10 to 15% • Long-term follow-up recommended

Odontogenic Myxoma

Etiology • A benign odontogenic tumor • Unknown origin


A lesion of adulthood (average occurrence at 30 years)

• Equal male:female and mandible:maxilla occurrences

• Wide age range: second through sixth decades

• Usually asymptomatic • May produce jaw expansion


Well-defined, unilocular to multilocular radiolucency

• Loculi range from small “honeycomb” to large “soap bubble”

shapes • Cortical thinning may be present with

larger lesions. • Perforation of the cortex is

uncommon.


Minimal cellularity, myxoid background

• Variable amounts of collagen • Scattered residual bony

trabeculae • Odontogenic epithelial rests are

rarely noted.

Diagnosis

Radiographic features • Microscopic findings


Other odontogenic tumor: ameloblastoma

• Odontogenic cysts: odontogenic keratocyst, dentigerous cyst,

glandular odontogenic cyst • Central giant cell granuloma

Treatment

Excision with bony curettage • Large lesions may require en bloc resection.

Prognosis

Good • Can be aggressive rarely • Recurrences not uncommon,

secondary to gelatinous quality and lack of capsule

Odontoma

Etiology • A hamartomatous or benign

mixed odontogenic tumor of the jaw

• Composed of enamel, dentin, cementum, and pulp tissue


Two forms, as follows: • Complex: a randomly arrayed mixture of dental

tissues with no gross resemblance to a tooth • Compound: multiple, tooth-like structures • Mean age of occurrence, 12 to 16 years • Asymptomatic, usually small and discovered

incidentally • Jaw expansion may be present with large lesions. • Presence may be heralded by an over-retained

primary tooth or by alveolar swelling.


Well-localized, mixed radiolucent and radiopaque lesion

• Within alveolar segment of jaws • Complex form most commonly noted

in mandibular molar area • Compound form favors anterior jaw

region, usually the maxilla; may contain a few small teeth or large

numbers of tiny tooth-like structures

Diagnosis

Radiographic presentation • Histologic demonstration of dental hard tissues


Ameloblastic fibro-odontoma • Adenomatoid odontogenic

tumor • Calcifying odontogenic cyst • Focal sclerosing osteitis,

osteoma

Treatment

Conservative excision/ curettage

Prognosis

Excellent

Peripheral Odontogenic Fibroma

Etiology • A benign Proliferation neoplasm of fibroblastic and odontogenic epithelial origin


Asymptomatic, firm, slow-growing mass of the attached gingiva

• Overlying mucosa unremarkable and intact • Sessile growth pattern • Usually along facial or buccal aspect of

gingiva • Calcifications may be present

radiographically. • Underlying alveolar bone is spared. • Uncommon to rare • Also seen centrally (within bone)

Diagnosis

Fibrous to myxoid stromal tissue • Scattered islands and strands of

odontogenic epithelium • Some cells may be vacuolated. • The degree of epithelial

proliferation may vary from minimal

to prominent.


Peripheral giant cell granuloma • Pyogenic granuloma • Peripheral fibroma • Peripheral ameloblastoma

Treatment

Excision: local and

conservative

Prognosis

Excellent

Odontogenic TumorsOdontogenic Tumors

Documents

Radiodiagnosis of dontogenous tumours and non tumoral formations of jaws. Radio diagnosis of non dontogenous benign and malignant tumours and non tumoral